Disposable Silicone Foley Catheter Three-way 22Fr

GUDID 26938634494934

Guangdong Baihe Medical Technology Co., Ltd.

Indwelling urethral drainage catheter

• Primary Device ID: 26938634494934
• NIH Device Record Key: 2a545e4d-3b52-4793-89c0-2588d43eca84
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Disposable Silicone Foley Catheter Three-way 22Fr
• Version Model Number: 110-FX-032240
• Company DUNS: 547055364
• Company Name: Guangdong Baihe Medical Technology Co., Ltd.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: true
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	06938634494930 [Primary]
GS1	16938634494937 [Package]; Contains: 06938634494930; Package: [10 Units]; In Commercial Distribution
GS1	26938634494934 [Package]; Contains: 16938634494937; Package: [200 Units]; In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K130908

FDA Product Code

• EZL: Catheter, Retention Type, Balloon

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: true

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 6
• Public Version Date: 2018-09-24
• Device Publish Date: 2016-09-20

On-Brand Devices [Disposable Silicone Foley Catheter Three-way 22Fr]

• 26938634494934: 110-FX-032240
• 26938634494927: 050-FX-032240